Biological Sciences Guidance on Data Management Plans

On October 1st, 2015, BIO made available an updated version of “Biological Sciences Guidance on Data Management Plans.”

A Data Management Plan (DMP) must be included with a full proposal and should describe how a project will conform to NSF policy on the dissemination and sharing of research results (see NSF 15-1 and NSF 16-1). The DMP is evaluated as part of the Merit Review process, either under the Intellectual Merit or the Broader Impacts criterion, or both, as appropriate for the scientific community of relevance. BIO anticipates differences in data management practices across the many research communities we support and recognizes that not all data are appropriate for post-project dissemination or preservation.

Generally, the DMP addresses two different aspects of the research process:

  • data handling during the project (which concerns robust and reliable research), and
  • preparation of data (software/materials/etc.) for dissemination or deposit for future access.

In brief, a DMP should include:

  • the types of data, samples, physical collections, software, curriculum and other materials to be produced in the course of the project;
  • standards to be used to contain and describe those data and materials, including (data) format and metadata standard;
  • policies that pertain to sharing and access, including where appropriate, consideration of
    • appropriate protection of privacy, confidentiality, security, intellectual property, or other rights or requirements; and
    • allowances or restrictions on re-use, re-distribution, and the production of derivatives;
  • plans for depositing or archiving data, samples, and other research products to preserve access to them.

In response to consultations with the scientific community and BIO’s Program Officers about data management, this updated BIO Guidance on DMPs is intended to clarify several required components identified in NSF policy. Please note that program-level data management requirements may be more specific or extensive than the BIO Guidance on DMPs, and you are advised to contact a BIO Program Officer if you have any questions related to a DMP in the program context.

Future blog posts will address BIOData as well as changes in the newly released version of the NSF Proposal & Award Policies & Procedures Guide (PAPPG; NSF 16-1); the new PAPPG is effective for proposals submitted, or due, on or after January 25, 2016.

BIO AD Testifies Before the House Committee on Appropriations regarding Federal Investments in Neuroscience and Neurotechnology

On March 26, 2015, Dr. James Olds testified before the Committee on Appropriations Subcommittee on Commerce, Justice, Science and Related Agencies, United States House of Representatives, on Federal Investments in Neuroscience and Neurotechnology.

Testimony Overview

The human brain is arguably the most complicated biological entity we are aware of in the universe. With roughly 100 billion neurons and 100 trillion synaptic connections linking them together, the brain is responsible not only for controlling basic physiology, such as breathing, but also for higher-level functions such as learning, memory, emotions and cognition.

NSF’s goal is to enable scientific understanding of the full complexity of the brain in action and in context. In order to meet this goal, fundamental research is needed to explore and discover the general principles underlying how cognition and behavior relate to the brain’s structural organization and dynamic activities, how the brain interacts with its environment, and how the brain can recover from lost functionality.

To address these issues, NSF is supporting interdisciplinary teams to develop the needed tools and to integrate their respective scientific disciplines at a rate they have not done in the past. NSF is strategically targeting its resource investments to advance the basic research needed to understand how healthy brains work and how they achieve cognition. An improved understanding of the healthy human brain is essential for dealing with the increasing frequency of neurological disorders that affect the human population.

Read more…

The Science and Ethics of Genetically Engineered Human DNA (House Subcommittee Hearing)

On Jun 16, 2015, at 2:00pm the House Subcommittee on Research and Technology will hold a hearing on The Science and Ethics of Genetically Engineered Human DNA

Opening Statements
Subcommittee on Research and Technology Chairwoman Barbara Comstock

Witnesses
Dr. Victor J. Dzau, President, Institute of Medicine, the National Academy of Sciences
Dr. Jennifer Doudna, Professor of Biochemistry and Molecular Biology, University of California, Berkeley
Dr. Elizabeth McNally, Professor of Genetic Medicine, Professor in Medicine-Cardiology and Biochemistry and Molecular Genetics; Director, Center for Genetic Medicine, Northwestern University
Dr. Jeffrey Kahn, Professor of Bioethics and Public Policy; Deputy Director for Policy and Administration, Berman Institute of Bioethics, Johns Hopkins University

Webcast: http://science.house.gov/hearing/subcommittee-research-and-technology-hearing-science-and-ethics-genetically-engineered-human

NSF’s Public Access Plan

The National Science Foundation has developed a plan outlining a framework for activities to increase public access to scientific publications and digital scientific data resulting from research the foundation funds. The plan, entitled “Today’s Data, Tomorrow’s Discoveries,” is consistent with the objectives set forth in the Office of Science and Technology Policy’s Feb. 22, 2013, memorandum, “Increasing Access to the Results of Federally Funded Research,” and with long-standing policies encouraging data sharing and communication of research results.

Read more…


Update 2/22/16

From The White House Blog (2/22/16): Increasing Access to the Results of Federally Funded Science